Canonical Allele Identifier: CA378126741

Gene: ABCC2

Linked Data

• MyVariant Identifiers: chr10:g.101604127G>T (hg19) ; chr10:g.99844370G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.99844370G>T , CM000672.2:g.99844370G>T	GRCh38
NC_000010.10:g.101604127G>T , CM000672.1:g.101604127G>T	GRCh37
NC_000010.9:g.101594117G>T	NCBI36
NG_011798.1:g.66665G>T
NG_011798.2:g.66773G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647814.1:c.3892G>T MANE Select	ENSP00000497274.1:p.Gly1298Cys
ENST00000649459.1:n.240G>T
ENST00000370449.8:c.3892G>T	ENSP00000359478.4:p.Gly1298Cys
NM_000392.4:c.3892G>T	NP_000383.1:p.Gly1298Cys
XM_006717630.2:c.3196G>T	XP_006717693.1:p.Gly1066Cys
XR_945604.1:n.4081G>T
XR_945605.1:n.3956G>T
NM_000392.5:c.3892G>T MANE Select	NP_000383.2:p.Gly1298Cys
XM_006717630.3:c.3196G>T	XP_006717693.1:p.Gly1066Cys
XR_945604.3:n.4135G>T
XR_945605.3:n.4008G>T